41994-91-6

Basic information

• Product Name: Benzamide, 4-chloro-2-nitro-
• CAS NO: 41994-91-6
• Molecular Formula: C7H5ClN2O3
• Molecular Weight: 200.581
• Mol File: 41994-91-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzamide, 4-chloro-2-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, 4-chloro-2-nitro-(41994-91-6)
• EPA Substance Registry System: Benzamide, 4-chloro-2-nitro-(41994-91-6)

Safety Data

• Hazardous Substances Data: 41994-91-6(Hazardous Substances Data)

Upstream product

• 34662-32-3 4-chloro-2-nitrobenzonitrile 
• 41995-04-4 4-chloro-2-nitro-benzoyl chloride 
• 6280-88-2 4-chloro-2-nitro-benzoic acid 

Downstream Products

• 1234324-11-8 7-chloro-2-(2-ethoxyethyl)-2-phenyl-2,3-dihydroquinazolin-4(1H)-one 
• 1234324-32-3 ethyl 4-(7-chloro-4-oxo-2-phenyl-1,2,3,4-tetrahydroquinazolin-2-yl)butanoate 
• 1234324-40-3 C₂₃H₂₇ClN₂O₃ 
• 1234324-38-9 C₂₂H₂₅ClN₂O₃ 
• 1234324-36-7 C₂₁H₂₃ClN₂O₃ 
• 118449-37-9 7-chloro-3-(4-chlorophenyl)-2-thioxo-2,3-dihydroquinazolin-4(1H)-one 
• 5900-59-4 2-amino-4-chlorobenzamide 
• 861603-76-1 4,4'-dichloro-2,2'-hydrazo-di-benzoic acid 
• 156149-37-0 2-azido-4-chlorobenzonitrile 
• 150097-32-8 4-amino-7-chloro-3-(3-phenoxyphenyl)quinolin-2(1H)-one 
• 38487-86-4 2-amino-4-chlorobenzonitrile 
• 13165-35-0 7-chloroquinazoline-2,4-dione 
• 34662-32-3 4-chloro-2-nitrobenzonitrile 
• 6280-88-2 4-chloro-2-nitro-benzoic acid 

Relevant articles and documents

Formamide as an ammonia synthon in amination of acid chlorides

The use of formamide as a convenient source of ammonia has been explored for the direct transformation of acid chlorides to primary amides. Various aliphatic, alicyclic aromatic, and heterocyclic acid chlorides are converted to the corresponding carboxamides in good yields (75-94%). Copyright Taylor & Francis Group, LLC.

3H-azepines and related systems. Part 5. Photo-induced ring expansions of o-azidobenzonitriles to 3-cyano- and 7-cyano-3H-azepin-2(1H)-ones

Unlike other aryl azides bearing electron-withdrawing ortho-substituents, o-azidobenzonitriles on photolysis in aqueous-tetrahydrofuran yield mixtures of the expected 3-cyano- and the unexpected 7-cyano-3H-azepin-2(1H)-ones. In one instance ring contraction to a 2-azabicyclo[3.2.0]hept-6-ene-3-one is noted. X-ray crystallographic data for 7-cyano- and 4-chloro-7-cyano-3H-azepin-2-one, and for the azabicycloheptenone, are presented.

1,2,3-Benzotriazin-4-ones and related systems. Part II. Thermolytic decomposition of substituted 1,2,3-benzotriazin-4-ones and isatoic anhydrides

Several nuclear-substituted 1,2,3-benzotriazin-4-ones have been thermolysed in an inert solvent. In each case the major identifiable product proved to be a 2-(o-aminophenyl)-3,1-benzoxazin-4-one. Nuclear-substituted isatoic anhydrides on thermolysis behaved similarly.